Ceppellini M
G Batteriol Virol Immunol. 1976 Jan-Jun;69(1-6):39-48.
The recent advances in the understanding of the Major Histocompatibility Complex, particularly of human HLA and murine H2, are critically reviewed. Special emphasis has been given to the new hypotheses regarding MHC a "rejection" system for recognizing and eliminating cells that have been altered in the expression of their so called transplantation antigens by viral infection or oncogenic transformation. Because Ir genes are certainly involved in controlling the immune response against modified autologous MHC antigens, the author forwards an original hypothesis for explaining the linkage disequilibrium between different alleles at the HLA: A, B, C loci: the Ir gene (genes) in a given haplotype is particularly efficient for recognizing some particular altered antigens of different serie (say A1 and B8; A3 and B7). If these is the case the Ir gene (genes) would be the Keystone for maintaining the preferential associations of some pseudoalleles in some haplotypes.
本文对主要组织相容性复合体,特别是人类HLA和小鼠H2的最新研究进展进行了批判性综述。特别强调了关于MHC作为一种“排斥”系统的新假说,该系统用于识别和消除因病毒感染或致癌转化而使其所谓移植抗原表达发生改变的细胞。由于Ir基因肯定参与了对修饰的自身MHC抗原的免疫反应控制,作者提出了一个原创假说来解释HLA的A、B、C位点不同等位基因之间的连锁不平衡:给定单倍型中的Ir基因(多个基因)对于识别不同系列的某些特定改变抗原(如A1和B8;A3和B7)特别有效。如果是这种情况,Ir基因(多个基因)将是维持某些单倍型中一些假等位基因优先关联的关键因素。